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Phoenix KinetiCream Anti-inflammatory and Pain Relief
Phoenix KinetiCream Anti-inflammatory and Pain Relief - 65121-032-04 - (MENTHOL)
Drug Information of Phoenix KinetiCream Anti-inflammatory and Pain Relief
| Product NDC: | 65121-032 |
| Proprietary Name: | Phoenix KinetiCream Anti-inflammatory and Pain Relief |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 20 mg/mL & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phoenix KinetiCream Anti-inflammatory and Pain Relief
| Product NDC: | 65121-032 |
| Labeler Name: | Pure Source, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130522 |
Package Information of Phoenix KinetiCream Anti-inflammatory and Pain Relief
| Package NDC: | 65121-032-04 |
| Package Description: | 118 mL in 1 TUBE (65121-032-04) |
NDC Information of Phoenix KinetiCream Anti-inflammatory and Pain Relief
| NDC Code | 65121-032-04 |
| Proprietary Name | Phoenix KinetiCream Anti-inflammatory and Pain Relief |
| Package Description | 118 mL in 1 TUBE (65121-032-04) |
| Product NDC | 65121-032 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130522 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Pure Source, Inc. |
| Substance Name | MENTHOL |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
